US20120171109A1 - Random graphite and fabrication method thereof using graphene nanoribbon - Google Patents

Random graphite and fabrication method thereof using graphene nanoribbon Download PDF

Info

Publication number
US20120171109A1
US20120171109A1 US13/340,839 US201113340839A US2012171109A1 US 20120171109 A1 US20120171109 A1 US 20120171109A1 US 201113340839 A US201113340839 A US 201113340839A US 2012171109 A1 US2012171109 A1 US 2012171109A1
Authority
US
United States
Prior art keywords
graphite
random
graphene
xrd
random graphite
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
US13/340,839
Other versions
US8586000B2 (en
Inventor
Jae-Kap Lee
Jin-Sup WON
Bo-Bae LEE
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Korea Advanced Institute of Science and Technology KAIST
Original Assignee
Korea Advanced Institute of Science and Technology KAIST
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Korea Advanced Institute of Science and Technology KAIST filed Critical Korea Advanced Institute of Science and Technology KAIST
Assigned to KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY reassignment KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LEE, BO-BAE, LEE, JAE-KAP, WON, JIN-SUP
Publication of US20120171109A1 publication Critical patent/US20120171109A1/en
Application granted granted Critical
Publication of US8586000B2 publication Critical patent/US8586000B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/20Graphite
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/15Nano-sized carbon materials
    • C01B32/182Graphene
    • C01B32/194After-treatment
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J19/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J19/08Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor
    • B01J19/10Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing sonic or ultrasonic vibrations
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00Manufacture or treatment of nanostructures
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/20Graphite
    • C01B32/205Preparation
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/38Selection of substances as active materials, active masses, active liquids of elements or alloys
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2204/00Structure or properties of graphene
    • C01B2204/04Specific amount of layers or specific thickness
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2204/00Structure or properties of graphene
    • C01B2204/06Graphene nanoribbons
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/32Hydrogen storage

Definitions

  • This specification relates to a carbon material and a fabrication method thereof, and particularly, to random graphite comprising graphene layers, which are three-dimensionally random in the random graphite, and a fabrication method is thereof using graphene nanoribbons.
  • Crystalline structures of graphite are classified according to stacking structures of graphene layers ( FIGS. 1 and 2 ). Since graphite having an AB-stacked structure (hereinafter, referred to as AB graphite) was reported in 1924 [Bernal et al, Proc. Roy. Soc. London, Ser. A 106, 749-773 (1924)], AB graphite (inter-layer spacing is 3.35 ⁇ ) has been known as the unique crystalline graphite. Also, the present inventor et al have reported presence of AA′ graphite (inter-layer spacing is 3.43-3.44 ⁇ ) [Lee et al, The Journal of Chemical Physics 129, 234709 (2008)].
  • AA graphite having an AA-stacked structure can exist crystallographically .
  • AA graphite cannot exist in nature because the AA stacking of graphene layers is unstable energetically , and is temporarily observable when Li atoms are intercalated into AB-stacked graphite.
  • turbostratic graphite (inter-layer spacing is 3.41-3.45 ⁇ ) has been reported in 1942 [J. Biscoe et al, Journal of Applied Physics 13 (1942) 364], and it is commonly known that turbostratic graphite has a structure that graphene layers are stacked parallel without any structural regularity between the layers. That is, the graphene layers of turbostratic graphite are parallel, but rotated each other ( FIG. 2D ). Therefore, turbostratic graphite can exhibit a clear and strong ( 002 ) peak on an X-Ray diffraction (XRD) pattern.
  • XRD X-Ray diffraction
  • An aspect of the detailed description is to provide graphite with a new structure in which graphene layers are three-dimensionally random, and a fabrication method thereof at a low temperature as below 100° C.
  • a fabrication method for a random graphite according to the present disclosure may comprise (a) preparing graphene nanoribbons, (b) forming a graphene solution by distributing the graphene nanoribbons in an organic solvent, and (c) drying the graphene solution to fabricate random graphite.
  • FIG. 1 is a diagram of graphite which is composed of parallel graphene layers
  • FIG. 2 is diagram showing types of graphite reported which are determined by stacking structures of graphene layers, wherein (a) shows AA graphite, (b) shows AB graphite, (c) shows AA′ graphite and (d) shows turbostratic graphite;
  • FIG. 3 is a diagram showing steps of a fabrication process for random graphite according to the present disclosure, wherein (a) shows graphene, (b) shows graphene suspension, and (c) shows random graphite;
  • FIG. 4 is a diagram showing XRD patterns and structures, wherein (a) shows crystalline graphite, (b) shows graphene nanoribbon, and (c) shows random graphite of the present disclosure; and
  • FIG. 5 is a diagram showing a Transmission Electron Microscopic (TEM) image of random graphite according to the present disclosure.
  • Random graphite comprises graphene layers which exist three-dimensionally random.
  • An average inter-layer distance of the random graphite measured by an XRD analysis may be 3.48 ⁇ .
  • the spacing is between those of AB graphite (3.35 ⁇ ) and AA graphite (3.53 ⁇ ), and is larger than that of AA′ graphite, 3.43-3.44 ⁇ .
  • a fabrication method for random graphite according to the present disclosure may comprise three steps (see FIG. 3 ), (a) preparing graphene nanoribbons, (b) forming a graphene suspension by dispersing the graphene nanoribbons in an organic solvent, and (c) drying the suspension to fabricate random graphite containing graphene layers, which are three-dimensionally random.
  • the organic solvent may be any one of alcohol, acetone, DMF, and combinations thereof, and the graphene nanoribbons may be less than 20 nm in length.
  • the step (b) can be performed by an ultrasonic treatment to distribute fully the graphene nanoribbons in the solvent, and the step (c) may be performed at a temperature range between room temperature (20° C.) and 200° C.
  • the graphene nanoribbons as a basic material used in the present disclosure may be obtained by physical decomposition of graphite in a shape of a helix (composed of graphene helices).
  • the graphene nanoribbons may be less is than 0.4 nm in thickness (namely, pure graphene), and less than 5 nm in width, less than 20 nm in length (generally less than 10 nm).
  • the presence of the graphene nanoribbons can be confirmed by XRD analysis, shown in (a) and (b) of FIG. 4 .
  • the sharp ( 002 ) peak of (a) in FIG. 4 exhibited in the crystalline graphite became broadened, demonstrating that the graphene layers of the ordered structure (a) were decomposed and scattered randomly.
  • the thusly-prepared graphene nanoribbons are uniformly distributed in an organic solvent 2 to create a distributed solution (graphene suspension).
  • the following embodiment has used alcohol as the organic solvent, but the present disclosure may not be limited to that.
  • An ultrasonic treatment may be performed for the distributed solution, thereby preparing a distributed solution in which the graphene nanoribbons are uniformly distributed in the alcohol ((b) of FIG. 3 ).
  • (A′) and (B′) of FIG. 3 are photos of distributed solutions, respectively, fabricated by distributing the prepared graphene nanoribbons into the organic solvent.
  • Random graphite comprises graphene layers, which are three-dimensionally random, like the case in the suspension ((c) of FIG. 3 ).
  • the temperature for drying the graphene suspension is not an important variable.
  • the samples can be dried in a conventional oven where available temperatures range between room temperature (20° C.) and 200° C.
  • the characteristic of the random graphite of the present disclosure is that a d (002) value of the ( 002 ) peak in the XRD is about 3.48 ⁇ , namely, larger than is that of the crystalline graphite (3.35-3.45 ⁇ ).
  • the randomly stacked graphene nanoribbons partially have AB, AA′ and AA stacked structures (each theoretical stacked distance, namely, d (002) is 3.35 ⁇ , 3.43 ⁇ and 3.53 ⁇ ), accordingly, the value may be predictable from an average value of the stacked distances.
  • the graphene nanoribbons three-dimensionally randomly exist in the random graphite, but the random graphite can have every type of stacked structure of AB, AA′, AA (graphene is slid) or turbostratic (graphene is rotated). Also, since the graphene nanoribbons are present randomly, the random graphite can have a space less than 1 nm (see 8 ⁇ indicated at the left of the ( 002 ) peak in (c) of FIG. 4 ). Of course, the random graphite may also partially have an empty space broader than 1 nm. Another characteristic of random graphite is that the ( 002 ) peak in the XRD pattern, as shown in (c) of FIG. 4 , is asymmetric.
  • the method may further comprise (d) performing a post-heat treatment for the random graphite at temperature lower than 1500° C. after the step (c). The additional post-heat treatment may improve crystallinity of graphene sheets comprising random graphite
  • Random graphite may have a large volume of an empty space due to the feature of the presence of the three-dimensionally random graphene nanoribbons.
  • GIC Graphitic Intercalation Compound
  • FIG. 4 the d-value of the asymmetric ( 002 ) peakly was measured to be 3.48 ⁇ .
  • a Transmission Electron Microscopic (TEM) analysis of the random graphite showed that graphene layers less than several nm in length were randomly present (also, graphene layers stacked in parallel are observable partially). Grain boundaries were not observed.
  • the XRD and TEM data demonstrate that the material is random graphite. There were no XRD and morphological changes with increasing the drying temperatures of the graphene suspension from the room temperature to 250° C.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nanotechnology (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Geology (AREA)
  • Materials Engineering (AREA)
  • Composite Materials (AREA)
  • Manufacturing & Machinery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Electrochemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Carbon And Carbon Compounds (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

Random graphite which is a type of graphite comprising three-dimensionally random graphene layers, and a fabrication method thereof at a low temperature as below 100° C. are disclosed. Random graphite may have a large volume of an empty space due to the feature of the presence of the three-dimensionally random graphene nanoribbons. Thus, it can be applied to Graphitic Intercalation Compound (GIC) such as electrodes for Li-ion battery.

Description

    CROSS-REFERENCE TO RELATED APPLICATION
  • The present disclosure relates to subject matter contained in priority Korean Application No. 10-2010-0139525, filed on Dec. 30, 2011, which is herein expressly incorporated by reference in its entirety.
  • BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • This specification relates to a carbon material and a fabrication method thereof, and particularly, to random graphite comprising graphene layers, which are three-dimensionally random in the random graphite, and a fabrication method is thereof using graphene nanoribbons.
  • 2.Background of the Invention
  • Crystalline structures of graphite are classified according to stacking structures of graphene layers (FIGS. 1 and 2). Since graphite having an AB-stacked structure (hereinafter, referred to as AB graphite) was reported in 1924 [Bernal et al, Proc. Roy. Soc. London, Ser. A 106, 749-773 (1924)], AB graphite (inter-layer spacing is 3.35 Å) has been known as the unique crystalline graphite. Also, the present inventor et al have reported presence of AA′ graphite (inter-layer spacing is 3.43-3.44 Å) [Lee et al, The Journal of Chemical Physics 129, 234709 (2008)].
  • AA graphite having an AA-stacked structure (theoretical inter-layer spacing is about 3.53 Å) can exist crystallographically . However, AA graphite cannot exist in nature because the AA stacking of graphene layers is unstable energetically , and is temporarily observable when Li atoms are intercalated into AB-stacked graphite.
  • Meanwhile, turbostratic graphite (inter-layer spacing is 3.41-3.45 Å) has been reported in 1942 [J. Biscoe et al, Journal of Applied Physics 13 (1942) 364], and it is commonly known that turbostratic graphite has a structure that graphene layers are stacked parallel without any structural regularity between the layers. That is, the graphene layers of turbostratic graphite are parallel, but rotated each other (FIG. 2D). Therefore, turbostratic graphite can exhibit a clear and strong (002) peak on an X-Ray diffraction (XRD) pattern.
  • All types of graphite reported previously, as shown in FIG. 1, are building blocks of parallel stacked graphene layers which are slid (AB, AA and AA′ graphites) or rotated (turbostratic graphite) and show a typical X-ray diffraction (XRD) pattern where a clear and strong (002) peak appears at 2θ=25.9° to 26.6°. This is the reason why graphite is named as an layered material. Meanwhile, amorphous carbon (or amorphous graphite) can be defined as a graphitic material in which graphene layers are not developed (thus, all XRD signals including (200) peaks are). All types of crystalline graphite are typically fabricated at a high temperature over about 2000° C.
  • SUMMARY OF THE INVENTION
  • An aspect of the detailed description is to provide graphite with a new structure in which graphene layers are three-dimensionally random, and a fabrication method thereof at a low temperature as below 100° C.
  • To achieve these and other advantages and in accordance with the purpose of this specification, as embodied and broadly described herein, there is provided random graphite where graphene layers exist disorderly three-dimensionally.
  • A fabrication method for a random graphite according to the present disclosure may comprise (a) preparing graphene nanoribbons, (b) forming a graphene solution by distributing the graphene nanoribbons in an organic solvent, and (c) drying the graphene solution to fabricate random graphite.
  • Further scope of applicability of the present application will become more apparent from the detailed description given hereinafter. However, it should be understood that the detailed description and specific examples, while indicating preferred embodiments of the invention, are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from the detailed description.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The accompanying drawings, which are included to provide a further understanding of the invention and are incorporated in and constitute a part of this specification, illustrate exemplary embodiments and together with the description serve to explain the principles of the invention.
  • In the drawings:
  • FIG. 1 is a diagram of graphite which is composed of parallel graphene layers;
  • FIG. 2 is diagram showing types of graphite reported which are determined by stacking structures of graphene layers, wherein (a) shows AA graphite, (b) shows AB graphite, (c) shows AA′ graphite and (d) shows turbostratic graphite;
  • FIG. 3 is a diagram showing steps of a fabrication process for random graphite according to the present disclosure, wherein (a) shows graphene, (b) shows graphene suspension, and (c) shows random graphite;
  • FIG. 4 is a diagram showing XRD patterns and structures, wherein (a) shows crystalline graphite, (b) shows graphene nanoribbon, and (c) shows random graphite of the present disclosure; and
  • FIG. 5 is a diagram showing a Transmission Electron Microscopic (TEM) image of random graphite according to the present disclosure.
  • DETAILED DESCRIPTION OF THE INVENTION
  • Random graphite according to the present disclosure comprises graphene layers which exist three-dimensionally random. An average inter-layer distance of the random graphite measured by an XRD analysis may be 3.48 Å. The spacing is between those of AB graphite (3.35 Å) and AA graphite (3.53 Å), and is larger than that of AA′ graphite, 3.43-3.44 Å.
  • The (002) peak in the XRD pattern for random graphite appears at 2θ=25.6° and may be asymmetric (See, the graph of FIG. 4).
  • A fabrication method for random graphite according to the present disclosure may comprise three steps (see FIG. 3), (a) preparing graphene nanoribbons, (b) forming a graphene suspension by dispersing the graphene nanoribbons in an organic solvent, and (c) drying the suspension to fabricate random graphite containing graphene layers, which are three-dimensionally random.
  • The organic solvent may be any one of alcohol, acetone, DMF, and combinations thereof, and the graphene nanoribbons may be less than 20 nm in length.
  • The step (b) can be performed by an ultrasonic treatment to distribute fully the graphene nanoribbons in the solvent, and the step (c) may be performed at a temperature range between room temperature (20° C.) and 200° C.
  • Hereinafter, each step will be described in more detail.
  • The graphene nanoribbons as a basic material used in the present disclosure may be obtained by physical decomposition of graphite in a shape of a helix (composed of graphene helices). The graphene nanoribbons may be less is than 0.4 nm in thickness (namely, pure graphene), and less than 5 nm in width, less than 20 nm in length (generally less than 10 nm). The presence of the graphene nanoribbons can be confirmed by XRD analysis, shown in (a) and (b) of FIG. 4. The sharp (002) peak of (a) in FIG. 4 exhibited in the crystalline graphite became broadened, demonstrating that the graphene layers of the ordered structure (a) were decomposed and scattered randomly.
  • The thusly-prepared graphene nanoribbons are uniformly distributed in an organic solvent 2 to create a distributed solution (graphene suspension). The following embodiment has used alcohol as the organic solvent, but the present disclosure may not be limited to that. An ultrasonic treatment may be performed for the distributed solution, thereby preparing a distributed solution in which the graphene nanoribbons are uniformly distributed in the alcohol ((b) of FIG. 3). (A′) and (B′) of FIG. 3 are photos of distributed solutions, respectively, fabricated by distributing the prepared graphene nanoribbons into the organic solvent.
  • Upon drying the graphene suspension, the graphene nanoribbons, which were randomly suspended in the solvent, are closely adhered each other by a strong surface tension (affinity) 3 of alcohol between graphene sheets, keeping a theoretical distance, thereby forming “random graphite”. Random graphite comprises graphene layers, which are three-dimensionally random, like the case in the suspension ((c) of FIG. 3).(
    Figure US20120171109A1-20120705-P00001
    Figure US20120171109A1-20120705-P00002
    Figure US20120171109A1-20120705-P00003
    )
  • In the meantime, the temperature for drying the graphene suspension is not an important variable. The samples can be dried in a conventional oven where available temperatures range between room temperature (20° C.) and 200° C.
  • The characteristic of the random graphite of the present disclosure is that a d(002) value of the (002) peak in the XRD is about 3.48 Å, namely, larger than is that of the crystalline graphite (3.35-3.45 Å). The randomly stacked graphene nanoribbons partially have AB, AA′ and AA stacked structures (each theoretical stacked distance, namely, d(002) is 3.35 Å, 3.43 Å and 3.53 Å), accordingly, the value may be predictable from an average value of the stacked distances. That is, the graphene nanoribbons three-dimensionally randomly exist in the random graphite, but the random graphite can have every type of stacked structure of AB, AA′, AA (graphene is slid) or turbostratic (graphene is rotated). Also, since the graphene nanoribbons are present randomly, the random graphite can have a space less than 1 nm (see 8 Å indicated at the left of the (002) peak in (c) of FIG. 4). Of course, the random graphite may also partially have an empty space broader than 1 nm. Another characteristic of random graphite is that the (002) peak in the XRD pattern, as shown in (c) of FIG. 4, is asymmetric. The method may further comprise (d) performing a post-heat treatment for the random graphite at temperature lower than 1500° C. after the step (c). The additional post-heat treatment may improve crystallinity of graphene sheets comprising random graphite
  • Random graphite may have a large volume of an empty space due to the feature of the presence of the three-dimensionally random graphene nanoribbons. Thus, it can be applied to Graphitic Intercalation Compound (GIC) such as electrodes for Li-ion battery.
  • EXAMPLE
  • Hereinafter, the example of the present disclosure will be described in detail. Here, the example may be merely illustrative to help easier understanding of the present disclosure, and the present disclosure may not be limited to the example.
  • Example 1
  • After preparing 5 g of graphene nanoribbons (i.e., pure graphene with a thickness of ˜0.4 nm) which were less than 5 nm in width and less than 10 nm in length, the graphene nanoribbons were put into 1000 cc of alcohol, followed by an ultrasonic treatment for 10 minutes, thereby creating a graphene suspension (a distributed state of this suspension was maintained for more than 3 months, and see (B′) of FIG. 3). This suspension was dried in a oven kept at 100° C.
  • The dried graphite material was black and exhibited a granular form with a size of several hundred μM, so it was similar to the existing graphite as it appeared. According to the XRD analysis (λ=1.541 Å) for this material, as shown in (c) of
  • FIG. 4, the d-value of the asymmetric (002) peakly was measured to be 3.48 Å. A Transmission Electron Microscopic (TEM) analysis of the random graphite showed that graphene layers less than several nm in length were randomly present (also, graphene layers stacked in parallel are observable partially). Grain boundaries were not observed. The XRD and TEM data demonstrate that the material is random graphite. There were no XRD and morphological changes with increasing the drying temperatures of the graphene suspension from the room temperature to 250° C.
  • The foregoing embodiments and advantages are merely exemplary and are not to be construed as limiting the present disclosure. The present teachings can be readily applied to other types of apparatuses. This description is intended to be illustrative, and not to limit the scope of the claims. Many alternatives, modifications, and variations will be apparent to those skilled in the art. The features, structures, methods, and other characteristics of the exemplary embodiments described herein may be combined in various ways to obtain additional and/or alternative exemplary embodiments.
  • As the present features may be embodied in several forms without departing from the characteristics thereof, it should also be understood that the above-described embodiments are not limited by any of the details of the foregoing description, unless otherwise specified, but rather should be construed broadly within its scope as defined in the appended claims, and therefore all changes and modifications that fall within the metes and bounds of the claims, or equivalents of such metes and bounds are therefore intended to be embraced by the appended claims.

Claims (11)

1. Random graphite which is a type of graphite comprising three-dimensionally random graphene layers.
2. The random graphite of claim 1, wherein an average inter-layer spacing measured by an X-ray diffraction (XRD) analysis for the random graphite is 3.48 Å.
3. The random graphite of claim 1, wherein an average 2θ value of a (002) peak by an XRD analysis (λ=1.541 Å) is 25.6°.
4. A method for fabricating random graphite comprising:
(a) preparing graphene nanoribbons;
(b) forming a graphene solution by dispersing the graphene nanoribbons in an organic solvent; and
(c) drying the graphene solution to fabricate a random graphite , wherein the graphene layers are three-dimensionally random.
5. The method of claim 4, wherein the organic solvent is alcohol, acetone, DMF, or combinations thereof.
6. The method of claim 4, wherein the graphene nanoribbon is shorter than 20 nm in length.
7. The method of claim 4, wherein the step (b) is performed by an ultrasonic treatment.
8. The method of claim 4, wherein the step (c) is performed at a temperature range between room temperature and 200° C.
9. The method of claim 4, comprising further step (d) after the step (c), and the step (d) is performing a post-heat treatment for the random graphite at temperature lower than 1500° C.
10. The method of claim 4, wherein an average inter-layer spacing measured by X-ray diffraction (XRD) analysis for the random graphite is 3.48 Å.
11. The method of claim 4, wherein an average 2θ value of a (002) peak by an XRD analysis (λ=1.541 Å) for the random graphite is 25.6°.
US13/340,839 2010-12-30 2011-12-30 Random graphite and fabrication method thereof using graphene nanoribbon Expired - Fee Related US8586000B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR10-2010-0139525 2010-12-30
KR1020100139525A KR101253050B1 (en) 2010-12-30 2010-12-30 Random graphite and the fabrication method thereof using graphene nanoribbon

Publications (2)

Publication Number Publication Date
US20120171109A1 true US20120171109A1 (en) 2012-07-05
US8586000B2 US8586000B2 (en) 2013-11-19

Family

ID=46380932

Family Applications (1)

Application Number Title Priority Date Filing Date
US13/340,839 Expired - Fee Related US8586000B2 (en) 2010-12-30 2011-12-30 Random graphite and fabrication method thereof using graphene nanoribbon

Country Status (2)

Country Link
US (1) US8586000B2 (en)
KR (1) KR101253050B1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103408004A (en) * 2013-08-02 2013-11-27 南京理工大学 Hydrophobic functional graphene oxide nano hybrid material with higher thermal stability and preparation method of hydrophobic functional graphene oxide nano hybrid material
CN111384395A (en) * 2020-03-20 2020-07-07 宁德新能源科技有限公司 Electrochemical device and electronic device
US11411222B2 (en) 2018-01-26 2022-08-09 Korea Advanced Institute Of Science And Technology Conductive agent, slurry for forming electrode including same, electrode, and lithium secondary battery manufactured using same

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015152483A1 (en) * 2014-04-02 2015-10-08 한국세라믹기술원 Graphene reference deriving method, nano thin film analysis method using same, x-ray analysis apparatus, and x-ray analysis method for graphene having extremely fine thickness
KR101494359B1 (en) * 2014-04-02 2015-02-24 한국세라믹기술원 Graphene reference inducing method & Nano-film analysis method using the same

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7094276B2 (en) * 2001-09-28 2006-08-22 Kabushiki Kaisha Toyota Chuo Kenkyusho Hydrogen storage material and hydrogen storage apparatus

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7094276B2 (en) * 2001-09-28 2006-08-22 Kabushiki Kaisha Toyota Chuo Kenkyusho Hydrogen storage material and hydrogen storage apparatus

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
Graphene Nanoribbon Thin Films Using Layer-by-Layer Assembly Yu Zhu and James M. Tour Nano Letters 2010 10 (11), 4356-4362 *
Jing Li, Jang-Kyo Kim, Percolation threshold of conducting polymer composites containing 3D randomly distributed graphite nanoplatelets, Composites Science and Technology, Volume 67, Issue 10, August 2007, Pages 2114-2120, ISSN 0266-3538, 10.1016/j.compscitech.2006.11.010.(http://www.sciencedirect.com/science/article/pii/S0266353806004386) *
Palser, Adam H. R.; "interlayer interactions in graphite and carbon nanotubes". Phys. Chem. Chem. Phys., 1999, 1, 4459-4464 *
Prudnikava et al. "Raman Characterization of Self-Organized Planar Graphite Layers on the top of Carbon Nanotube Arrays" PHYSICS, CHEMISTRY AND APPLICATION OF NANOSTRUCTURESReviews and Short Notes Proceedings of International Conference Nanomeeting. May 2011. *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103408004A (en) * 2013-08-02 2013-11-27 南京理工大学 Hydrophobic functional graphene oxide nano hybrid material with higher thermal stability and preparation method of hydrophobic functional graphene oxide nano hybrid material
CN103408004B (en) * 2013-08-02 2015-02-25 南京理工大学 Hydrophobic functional graphene oxide nano hybrid material with higher thermal stability and preparation method of hydrophobic functional graphene oxide nano hybrid material
US11411222B2 (en) 2018-01-26 2022-08-09 Korea Advanced Institute Of Science And Technology Conductive agent, slurry for forming electrode including same, electrode, and lithium secondary battery manufactured using same
CN111384395A (en) * 2020-03-20 2020-07-07 宁德新能源科技有限公司 Electrochemical device and electronic device

Also Published As

Publication number Publication date
KR20120077535A (en) 2012-07-10
US8586000B2 (en) 2013-11-19
KR101253050B1 (en) 2013-04-11

Similar Documents

Publication Publication Date Title
Anasori et al. 2D metal carbides and nitrides (MXenes) for energy storage
Shi et al. Recent advances in inorganic 2D materials and their applications in lithium and sodium batteries
Zhou et al. A two‐dimensional zirconium carbide by selective etching of Al3C3 from nanolaminated Zr3Al3C5
US20120171109A1 (en) Random graphite and fabrication method thereof using graphene nanoribbon
Ji et al. Porous hybrid composites of few‐layer MoS2 nanosheets embedded in a carbon matrix with an excellent supercapacitor electrode performance
Yang et al. Self‐Assembled α‐Fe2O3 mesocrystals/graphene nanohybrid for enhanced electrochemical capacitors
Sun et al. Carbon nanorings and their enhanced lithium storage properties
Sari et al. Direct growth of MoS2 nanowalls on carbon nanofibers for use in supercapacitor
Kim et al. Understanding excess Li storage beyond LiC6 in reduced dimensional scale graphene
Kumar et al. Direct synthesis of lithium-intercalated graphene for electrochemical energy storage application
Gong et al. A bottom‐up approach to build 3D architectures from nanosheets for superior lithium storage
Huang et al. Vanadium pentoxide‐based cathode materials for lithium‐ion batteries: morphology control, carbon hybridization, and cation doping
Zou et al. Carbon nanofibers: Synthesis, characterization, and electrochemical properties
Yoon et al. Low-dimensional carbon and MXene-based electrochemical capacitor electrodes
US9868640B2 (en) Graphene structure and method of manufacturing the same
Zhang et al. Large‐Scale Production of Nanographene Sheets with a Controlled Mesoporous Architecture as High‐Performance Electrochemical Electrode Materials
He et al. Engineering vertical aligned MoS2 on graphene sheet towards thin film lithium ion battery
Sreedhara et al. Atomic layer deposition of crystalline epitaxial MoS 2 nanowall networks exhibiting superior performance in thin-film rechargeable Na-ion batteries
Yao et al. Flexible α-MnO2 paper formed by millimeter-long nanowires for supercapacitor electrodes
Simon et al. Improving anodes for lithium ion batteries
Zhao et al. Electromagnetic wave absorbing properties of aligned amorphous carbon nanotube/BaFe12O19 nanorod composite
Yun et al. Restoration of thermally reduced graphene oxide by atomic-level selenium doping
Gu et al. Porous hybrid network of graphene and metal oxide nanosheets as useful matrix for improving the electrode performance of layered double hydroxides
JP2013527576A5 (en)
Wang et al. The study of carbon nanotubes as conductive additives of cathode in lithium ion batteries

Legal Events

Date Code Title Description
AS Assignment

Owner name: KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY, KOREA,

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LEE, JAE-KAP;WON, JIN-SUP;LEE, BO-BAE;REEL/FRAME:027462/0032

Effective date: 20111228

STCF Information on status: patent grant

Free format text: PATENTED CASE

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY

FPAY Fee payment

Year of fee payment: 4

FEPP Fee payment procedure

Free format text: MAINTENANCE FEE REMINDER MAILED (ORIGINAL EVENT CODE: REM.); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY

LAPS Lapse for failure to pay maintenance fees

Free format text: PATENT EXPIRED FOR FAILURE TO PAY MAINTENANCE FEES (ORIGINAL EVENT CODE: EXP.); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY

STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362

FP Lapsed due to failure to pay maintenance fee

Effective date: 20211119